| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:29850274-29850654 | Common:6; Rare:125 | ||||
| chr13:30306813-30307160 | Common:6; Rare:90 | ||||
| chr13:30617263-30617993 | Common:1; Rare:225 | ||||
| chr13:31162337-31162511 | Common:2; Rare:52 | ||||
| chr13:32031487-32031579 | Rare:18 | ||||
| chr13:32031581-32031774 | Common:1; Rare:53 | ||||
| chr13:32586260-32586612 | Common:2; Rare:107 | ||||
| chr13:33285657-33286017 | Common:1; Rare:77 | ||||
| chr13:33350599-33350872 | Rare:66 | ||||
| chr13:36346279-36346509 | Common:3; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:37000736-37000811 | Rare:31; Clinvar (pathogenic):1 | ||||
| chr13:38349544-38349974 | Common:4; Rare:151; Clinvar (pathogenic):1 | ||||
| chr13:39037866-39038443 | Common:2; Rare:156 | ||||
| chr13:39603114-39603284 | Common:1; Rare:56 | ||||
| chr13:40771135-40771347 | Common:3; Rare:70 |